Found 46 hits with Last Name = 'alao' and Initial = 'jp' Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196604
(CHEMBL217083 | N-hydroxy-7-(naphthalen-2-yloxy)hep...)Show InChI InChI=1S/C17H21NO3/c19-17(18-20)9-3-1-2-6-12-21-16-11-10-14-7-4-5-8-15(14)13-16/h4-5,7-8,10-11,13,20H,1-3,6,9,12H2,(H,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.900 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196608
(7-(4-((4-chlorobenzyl)(methyl)amino)phenoxy)-N-hyd...)Show InChI InChI=1S/C21H27ClN2O3/c1-24(16-17-7-9-18(22)10-8-17)19-11-13-20(14-12-19)27-15-5-3-2-4-6-21(25)23-26/h7-14,26H,2-6,15-16H2,1H3,(H,23,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196600
(7-(1H-indol-5-yloxy)-N-hydroxyheptanamide | CHEMBL...)Show InChI InChI=1S/C15H20N2O3/c18-15(17-19)5-3-1-2-4-10-20-13-6-7-14-12(11-13)8-9-16-14/h6-9,11,16,19H,1-5,10H2,(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 3.60 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50005711
(CHEBI:46024 | GNF-Pf-1011 | TRICHOSTATIN | Trichos...)Show SMILES C[C@H](\C=C(/C)\C=C\C(=O)NO)C(=O)c1ccc(cc1)N(C)C |r| Show InChI InChI=1S/C17H22N2O3/c1-12(5-10-16(20)18-22)11-13(2)17(21)14-6-8-15(9-7-14)19(3)4/h5-11,13,22H,1-4H3,(H,18,20)/b10-5+,12-11+/t13-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE PC cid PC sid PDB UniChem
| PDB PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196598
(7-(4-(3-(1H-indol-3-yl)prop-1-en-2-ylamino)phenyl1...)Show SMILES CC(Cc1c[nH]c2ccccc12)=Nc1ccc(OCCCCCCC(=O)NO)cc1 |w:12.14| Show InChI InChI=1S/C24H29N3O3/c1-18(16-19-17-25-23-9-6-5-8-22(19)23)26-20-11-13-21(14-12-20)30-15-7-3-2-4-10-24(28)27-29/h5-6,8-9,11-14,17,25,29H,2-4,7,10,15-16H2,1H3,(H,27,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.20 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50388620
(CHEMBL2058538)Show InChI InChI=1S/C16H15N5/c1-11(2)21-16-14(15(17)18-10-19-16)13(20-21)9-8-12-6-4-3-5-7-12/h3-7,10-11H,1-2H3,(H2,17,18,19) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of RET by commercial radiometric assay |
J Med Chem 55: 4872-6 (2012)
Article DOI: 10.1021/jm3003944 BindingDB Entry DOI: 10.7270/Q2NK3G3N |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196605
(7-(4-(2-(1H-indol-3-yl)acetamido)phenyl1H-indol-3-...)Show SMILES ONC(=O)CCCCCCOc1ccc(NC(=O)Cc2c[nH]c3ccccc23)cc1 Show InChI InChI=1S/C23H27N3O4/c27-22(26-29)9-3-1-2-6-14-30-19-12-10-18(11-13-19)25-23(28)15-17-16-24-21-8-5-4-7-20(17)21/h4-5,7-8,10-13,16,24,29H,1-3,6,9,14-15H2,(H,25,28)(H,26,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196603
(7-(4-(2-(1H-indol-3-yl)acetamido)-2-fluorophenyl1H...)Show SMILES ONC(=O)CCCCCCOc1ccc(NC(=O)Cc2c[nH]c3ccccc23)cc1F Show InChI InChI=1S/C23H26FN3O4/c24-19-14-17(10-11-21(19)31-12-6-2-1-3-9-22(28)27-30)26-23(29)13-16-15-25-20-8-5-4-7-18(16)20/h4-5,7-8,10-11,14-15,25,30H,1-3,6,9,12-13H2,(H,26,29)(H,27,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196594
(7-(4-((1H-indol-5-yl)methylamino)phenyl1H-indol-5-...)Show InChI InChI=1S/C22H27N3O3/c26-22(25-27)5-3-1-2-4-14-28-20-9-7-19(8-10-20)24-16-17-6-11-21-18(15-17)12-13-23-21/h6-13,15,23-24,27H,1-5,14,16H2,(H,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196597
(CHEMBL384714 | N-hydroxy-7-(4-(methyl(pyridin-4-yl...)Show InChI InChI=1S/C20H27N3O3/c1-23(16-17-11-13-21-14-12-17)18-7-9-19(10-8-18)26-15-5-3-2-4-6-20(24)22-25/h7-14,25H,2-6,15-16H2,1H3,(H,22,24) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196607
(7-(4-(3-(1H-indol-3-yl)-N-(pyridin-4-ylmethyl)prop...)Show SMILES ONC(=O)CCCCCCOc1ccc(cc1)N(Cc1ccncc1)C(=O)CCc1c[nH]c2ccccc12 Show InChI InChI=1S/C30H34N4O4/c35-29(33-37)9-3-1-2-6-20-38-26-13-11-25(12-14-26)34(22-23-16-18-31-19-17-23)30(36)15-10-24-21-32-28-8-5-4-7-27(24)28/h4-5,7-8,11-14,16-19,21,32,37H,1-3,6,9-10,15,20,22H2,(H,33,35) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196609
(7-(4-(3-(1H-indol-3-yl)propanamido)phenyl1H-indol-...)Show SMILES ONC(=O)CCCCCCOc1ccc(NC(=O)CCc2c[nH]c3ccccc23)cc1 Show InChI InChI=1S/C24H29N3O4/c28-23(15-10-18-17-25-22-8-5-4-7-21(18)22)26-19-11-13-20(14-12-19)31-16-6-2-1-3-9-24(29)27-30/h4-5,7-8,11-14,17,25,30H,1-3,6,9-10,15-16H2,(H,26,28)(H,27,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385649
(CHEMBL2041958)Show SMILES CC(C)Nc1cc(ccn1)-c1oc2ccccc2c(=O)c1-c1ccc(F)cc1 Show InChI InChI=1S/C23H19FN2O2/c1-14(2)26-20-13-16(11-12-25-20)23-21(15-7-9-17(24)10-8-15)22(27)18-5-3-4-6-19(18)28-23/h3-14H,1-2H3,(H,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196602
(7-(4-(dimethylamino)phenoxy)-N-hydroxyheptanamide ...)Show InChI InChI=1S/C15H24N2O3/c1-17(2)13-8-10-14(11-9-13)20-12-6-4-3-5-7-15(18)16-19/h8-11,19H,3-7,12H2,1-2H3,(H,16,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 19 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385650
(CHEMBL2041959)Show SMILES CCCCNc1cc(ccn1)-c1oc2ccccc2c(=O)c1-c1ccc(F)cc1 Show InChI InChI=1S/C24H21FN2O2/c1-2-3-13-26-21-15-17(12-14-27-21)24-22(16-8-10-18(25)11-9-16)23(28)19-6-4-5-7-20(19)29-24/h4-12,14-15H,2-3,13H2,1H3,(H,26,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 21 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196593
(CHEMBL387042 | N-hydroxy-7-(4-((3-hydroxy-5-(hydro...)Show InChI InChI=1S/C21H29N3O5/c1-15-21(27)19(16(14-25)12-22-15)13-23-17-7-9-18(10-8-17)29-11-5-3-2-4-6-20(26)24-28/h7-10,12,23,25,27-28H,2-6,11,13-14H2,1H3,(H,24,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196596
(8-(4-(2-(1H-indol-3-yl)acetamido)phenyl1H-indol-3-...)Show SMILES ONC(=O)CCCCCCCOc1ccc(NC(=O)Cc2c[nH]c3ccccc23)cc1 Show InChI InChI=1S/C24H29N3O4/c28-23(27-30)10-4-2-1-3-7-15-31-20-13-11-19(12-14-20)26-24(29)16-18-17-25-22-9-6-5-8-21(18)22/h5-6,8-9,11-14,17,25,30H,1-4,7,10,15-16H2,(H,26,29)(H,27,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196601
(CHEMBL217778 | N-hydroxy-7-(4-(4-methoxyphenylsulf...)Show SMILES COc1ccc(cc1)S(=O)(=O)Nc1ccc(OCCCCCCC(=O)NO)cc1 Show InChI InChI=1S/C20H26N2O6S/c1-27-17-11-13-19(14-12-17)29(25,26)22-16-7-9-18(10-8-16)28-15-5-3-2-4-6-20(23)21-24/h7-14,22,24H,2-6,15H2,1H3,(H,21,23) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196606
(7-(4-(2-(1H-indol-3-yl)acetamido)-3-fluorophenyl1H...)Show SMILES ONC(=O)CCCCCCOc1ccc(NC(=O)Cc2c[nH]c3ccccc23)c(F)c1 Show InChI InChI=1S/C23H26FN3O4/c24-19-14-17(31-12-6-2-1-3-9-22(28)27-30)10-11-21(19)26-23(29)13-16-15-25-20-8-5-4-7-18(16)20/h4-5,7-8,10-11,14-15,25,30H,1-3,6,9,12-13H2,(H,26,29)(H,27,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385653
(CHEMBL2041962)Show SMILES Fc1ccc(cc1)-c1c(oc2ccccc2c1=O)-c1ccnc(NC2CCCCC2)c1 Show InChI InChI=1S/C26H23FN2O2/c27-19-12-10-17(11-13-19)24-25(30)21-8-4-5-9-22(21)31-26(24)18-14-15-28-23(16-18)29-20-6-2-1-3-7-20/h4-5,8-16,20H,1-3,6-7H2,(H,28,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 34 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385654
(CHEMBL2042121)Show SMILES Fc1ccc(cc1)-c1c(oc2ccccc2c1=O)-c1ccnc(NCc2ccccc2)c1 Show InChI InChI=1S/C27H19FN2O2/c28-21-12-10-19(11-13-21)25-26(31)22-8-4-5-9-23(22)32-27(25)20-14-15-29-24(16-20)30-17-18-6-2-1-3-7-18/h1-16H,17H2,(H,29,30) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 35 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385651
(CHEMBL2041960)Show SMILES COCCCNc1cc(ccn1)-c1oc2ccccc2c(=O)c1-c1ccc(F)cc1 Show InChI InChI=1S/C24H21FN2O3/c1-29-14-4-12-26-21-15-17(11-13-27-21)24-22(16-7-9-18(25)10-8-16)23(28)19-5-2-3-6-20(19)30-24/h2-3,5-11,13,15H,4,12,14H2,1H3,(H,26,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 39 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50388621
(CHEMBL2058539)Show InChI InChI=1S/C16H14FN5/c1-10(2)22-16-14(15(18)19-9-20-16)13(21-22)8-5-11-3-6-12(17)7-4-11/h3-4,6-7,9-10H,1-2H3,(H2,18,19,20) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 43 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of RET by commercial radiometric assay |
J Med Chem 55: 4872-6 (2012)
Article DOI: 10.1021/jm3003944 BindingDB Entry DOI: 10.7270/Q2NK3G3N |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385646
(CHEMBL2041963)Show SMILES Fc1ccc(cc1)-c1c(oc2ccccc2c1=O)-c1ccnc(NC2CCOCC2)c1 Show InChI InChI=1S/C25H21FN2O3/c26-18-7-5-16(6-8-18)23-24(29)20-3-1-2-4-21(20)31-25(23)17-9-12-27-22(15-17)28-19-10-13-30-14-11-19/h1-9,12,15,19H,10-11,13-14H2,(H,27,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 45 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223405
(CHEMBL316183)Show SMILES C\C(\C=C\C(=O)NO)=C/c1ccc(NS(=O)(=O)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C18H17ClN2O4S/c1-13(2-11-18(22)20-23)12-14-3-7-16(8-4-14)21-26(24,25)17-9-5-15(19)6-10-17/h2-12,21,23H,1H3,(H,20,22)/b11-2+,13-12+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 49 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196595
(6-(4-(2-(1H-indol-3-yl)acetamido)phenyl1H-indol-3-...)Show SMILES ONC(=O)CCCCCOc1ccc(NC(=O)Cc2c[nH]c3ccccc23)cc1 Show InChI InChI=1S/C22H25N3O4/c26-21(25-28)8-2-1-5-13-29-18-11-9-17(10-12-18)24-22(27)14-16-15-23-20-7-4-3-6-19(16)20/h3-4,6-7,9-12,15,23,28H,1-2,5,8,13-14H2,(H,24,27)(H,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50388624
(CHEMBL2058543)Show InChI InChI=1S/C16H17N5/c1-11(2)21-16-14(15(17)18-10-19-16)13(20-21)9-8-12-6-4-3-5-7-12/h3-11H,1-2H3,(H2,17,18,19)/b9-8+ | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of RET by commercial radiometric assay |
J Med Chem 55: 4872-6 (2012)
Article DOI: 10.1021/jm3003944 BindingDB Entry DOI: 10.7270/Q2NK3G3N |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50196599
(7-(3-fluoro-4-((3-hydroxy-5-(hydroxymethyl)-2-meth...)Show SMILES Cc1ncc(CO)c(CNc2ccc(OCCCCCCC(=O)NO)cc2F)c1O Show InChI InChI=1S/C21H28FN3O5/c1-14-21(28)17(15(13-26)11-23-14)12-24-19-8-7-16(10-18(19)22)30-9-5-3-2-4-6-20(27)25-29/h7-8,10-11,24,26,28-29H,2-6,9,12-13H2,1H3,(H,25,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description In vitro inhibition of histone deacetylase activity using HeLa cell nuclear extract as enzyme source |
Bioorg Med Chem Lett 17: 136-41 (2006)
Article DOI: 10.1016/j.bmcl.2006.09.085 BindingDB Entry DOI: 10.7270/Q2B56JDQ |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223410
(CHEMBL82931)Show SMILES COc1ccc(cc1)S(=O)(=O)Nc1ccc(\C=C(/C)\C=C\C(=O)NO)cc1 Show InChI InChI=1S/C19H20N2O5S/c1-14(3-12-19(22)20-23)13-15-4-6-16(7-5-15)21-27(24,25)18-10-8-17(26-2)9-11-18/h3-13,21,23H,1-2H3,(H,20,22)/b12-3+,14-13+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 74 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50388625
(CHEMBL2058542)Show InChI InChI=1S/C18H19N5/c1-11(2)23-18-16(17(19)20-10-21-18)15(22-23)8-7-14-9-12(3)5-6-13(14)4/h5-6,9-11H,1-4H3,(H2,19,20,21) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 83 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of RET by commercial radiometric assay |
J Med Chem 55: 4872-6 (2012)
Article DOI: 10.1021/jm3003944 BindingDB Entry DOI: 10.7270/Q2NK3G3N |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50388622
(CHEMBL2058540)Show InChI InChI=1S/C16H16N6/c1-10(2)22-16-14(15(18)19-9-20-16)13(21-22)7-6-11-4-3-5-12(17)8-11/h3-5,8-10H,17H2,1-2H3,(H2,18,19,20) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of RET by commercial radiometric assay |
J Med Chem 55: 4872-6 (2012)
Article DOI: 10.1021/jm3003944 BindingDB Entry DOI: 10.7270/Q2NK3G3N |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223409
(CHEMBL314643)Show SMILES C\C(\C=C\C(=O)NO)=C/c1ccc(NS(=O)(=O)c2ccccc2)cc1 Show InChI InChI=1S/C18H18N2O4S/c1-14(7-12-18(21)19-22)13-15-8-10-16(11-9-15)20-25(23,24)17-5-3-2-4-6-17/h2-13,20,22H,1H3,(H,19,21)/b12-7+,14-13+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 172 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase receptor Ret
(Homo sapiens (Human)) | BDBM50388623
(CHEMBL2058541)Show InChI InChI=1S/C16H16N6/c1-10(2)22-16-14(15(18)19-9-20-16)13(21-22)8-7-11-5-3-4-6-12(11)17/h3-6,9-10H,17H2,1-2H3,(H2,18,19,20) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 195 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of RET by commercial radiometric assay |
J Med Chem 55: 4872-6 (2012)
Article DOI: 10.1021/jm3003944 BindingDB Entry DOI: 10.7270/Q2NK3G3N |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223408
(CHEMBL312098)Show InChI InChI=1S/C11H10ClNO2/c12-10-7-5-9(6-8-10)3-1-2-4-11(14)13-15/h1-8,15H,(H,13,14)/b3-1+,4-2+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 252 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223416
(CHEMBL84395)Show InChI InChI=1S/C11H11NO2/c13-11(12-14)9-5-4-8-10-6-2-1-3-7-10/h1-9,14H,(H,12,13)/b8-4+,9-5+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 279 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223411
(CHEMBL81522)Show InChI InChI=1S/C12H12ClNO2/c1-9(2-7-12(15)14-16)8-10-3-5-11(13)6-4-10/h2-8,16H,1H3,(H,14,15)/b7-2+,9-8+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 302 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385652
(CHEMBL2041961)Show SMILES CN(C)CCCNc1cc(ccn1)-c1oc2ccccc2c(=O)c1-c1ccc(F)cc1 Show InChI InChI=1S/C25H24FN3O2/c1-29(2)15-5-13-27-22-16-18(12-14-28-22)25-23(17-8-10-19(26)11-9-17)24(30)20-6-3-4-7-21(20)31-25/h3-4,6-12,14,16H,5,13,15H2,1-2H3,(H,27,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 761 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223407
(CHEMBL82989)Show InChI InChI=1S/C14H18N2O2/c1-11(4-9-14(17)15-18)10-12-5-7-13(8-6-12)16(2)3/h4-10,18H,1-3H3,(H,15,17)/b9-4+,11-10+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 788 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385647
(CHEMBL2041956)Show InChI InChI=1S/C20H12FNO2/c21-15-7-5-13(6-8-15)18-19(23)16-3-1-2-4-17(16)24-20(18)14-9-11-22-12-10-14/h1-12H | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 813 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223406
(CHEMBL312400)Show SMILES CC(CCC(=O)NO)Cc1ccc(NS(=O)(=O)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C18H21ClN2O4S/c1-13(2-11-18(22)20-23)12-14-3-7-16(8-4-14)21-26(24,25)17-9-5-15(19)6-10-17/h3-10,13,21,23H,2,11-12H2,1H3,(H,20,22) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.17E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50385648
(CHEMBL2041957)Show SMILES Fc1ccc(cc1)-c1c(oc2ccccc2c1=O)-c1ccnc(Cl)c1 Show InChI InChI=1S/C20H11ClFNO2/c21-17-11-13(9-10-23-17)20-18(12-5-7-14(22)8-6-12)19(24)15-3-1-2-4-16(15)25-20/h1-11H | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Gothenburg
Curated by ChEMBL
| Assay Description Inhibition of p38alpha MAPK after 40 mins by scintillation counting |
J Med Chem 54: 7427-31 (2011)
Article DOI: 10.1021/jm200818j BindingDB Entry DOI: 10.7270/Q2R78G7T |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223414
(CHEMBL83750)Show InChI InChI=1S/C13H16N2O2/c1-15(2)12-9-7-11(8-10-12)5-3-4-6-13(16)14-17/h3-10,17H,1-2H3,(H,14,16)/b5-3+,6-4+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50123957
((E)-5-(3-Benzenesulfonylamino-phenyl)-pent-2-en-4-...)Show SMILES ONC(=O)\C=C\C#Cc1ccc(NS(=O)(=O)c2ccccc2)cc1 Show InChI InChI=1S/C17H14N2O4S/c20-17(18-21)9-5-4-6-14-10-12-15(13-11-14)19-24(22,23)16-7-2-1-3-8-16/h1-3,5,7-13,19,21H,(H,18,20)/b9-5+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223412
(CHEMBL84288)Show InChI InChI=1S/C11H14ClNO2/c12-10-7-5-9(6-8-10)3-1-2-4-11(14)13-15/h5-8,15H,1-4H2,(H,13,14) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.58E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223413
(CHEMBL82382)Show SMILES COc1ccc(cc1)S(=O)(=O)Nc1ccc(\C=C\C=C\C(=O)NO)cc1 Show InChI InChI=1S/C18H18N2O5S/c1-25-16-10-12-17(13-11-16)26(23,24)20-15-8-6-14(7-9-15)4-2-3-5-18(21)19-22/h2-13,20,22H,1H3,(H,19,21)/b4-2+,5-3+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.04E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50223415
(CHEMBL312253)Show SMILES C\C(\C=C\C(O)=O)=C/c1ccc(NS(=O)(=O)c2ccc(Cl)cc2)cc1 Show InChI InChI=1S/C18H16ClNO4S/c1-13(2-11-18(21)22)12-14-3-7-16(8-4-14)20-25(23,24)17-9-5-15(19)6-10-17/h2-12,20H,1H3,(H,21,22)/b11-2+,13-12+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
University College London
Curated by ChEMBL
| Assay Description Inhibition of histone deacetylase (HDAC) activity in HeLa cell nuclear extract |
Bioorg Med Chem Lett 14: 2477-81 (2004)
BindingDB Entry DOI: 10.7270/Q2S184Q6 |
More data for this Ligand-Target Pair | |